Bioserenity Medical Devices Group

Bioserenity Medical Devices Group — FDA 510(k) Submissions

Bioserenity Medical Devices Group has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrode, Cutaneous . Use the specialty filter in the sidebar to narrow results.